Label: SUGAR BRANDS RESCUE PAIN RELIEF AND RECOVERY- lidocaine hydrochloride cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2023

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active Ingredient

    Lidocaine HCl 4.00%

    Purpose

    Topical Analgesic

  • Uses

    • For the temporary relief of pain
  • Warnings

    • For external use only.
    • Avoid contact with eyes.
    • If symptoms persist for more than seven days, discontinue use and consult physician.

    Keep out of reach of children.

    If swallowed, consult physician.

    Do not use 

    in large quantities, particularly over raw surfaces or blistered areas.

    If pregnant or breast feeding,

    contact physician prior to use.

  • Directions

    Adults and children two-years of age or older:

    • Apply to affected area not more than three to four times daily.
    • Children under two-years of age: consult a physician.
  • Additional Information

    Store at room temperature.

  • Other Ingredients

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aesculus Hippocastanum (Horse Chestnut) Extract, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Beta Alanine, Betaglucan, Boswellia Serrata Extract, Butyrospermum Parkii (Shea) Butter, Cannabis Sativa (Hemp) Seed Oil, Cetyl Esters, Dimethicone, Ethoxydiglycol, Ethylhexylglycerin, Ethyl Vanillin, Eucalyptus Globulus Oil, Glucosamine Sulfate, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, l-Arginine, l-Carnitine, l-Citruline, Magnesium Sulfate, Methyl Gluceth-20, Methylsulfonylmethane (MSM), PEG-100 Stearate, Phenoxyethanol, Ribes Nigrum (Black Currant) Oil, Salix Alba (Willow) Bark Extract, Steareth-20, Triethanolamine.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    SUGAR BRANDS RESCUE PAIN RELIEF AND RECOVERY 
    lidocaine hydrochloride cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73313-075
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    HORSE CHESTNUT (UNII: 3C18L6RJAZ)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    .BETA.-ALANINE (UNII: 11P2JDE17B)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    CETYL ESTERS WAX (UNII: D072FFP9GU)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ETHYL VANILLIN (UNII: YC9ST449YJ)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
    ARGININE (UNII: 94ZLA3W45F)  
    LEVOCARNITINE (UNII: 0G389FZZ9M)  
    CITRULLINE (UNII: 29VT07BGDA)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BLACK CURRANT (UNII: 9755T40D11)  
    SALIX ALBA BARK (UNII: 205MXS71H7)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73313-075-04118 mL in 1 TUBE; Type 0: Not a Combination Product08/20/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/20/2019
    Labeler - Sugar Brands, LLC (050377177)